Background: Sheep coccidiosis could disturb the balance of intestinal microbiota, causing diarrhea, and even death in lambs. Chemical drugs are the primary method of treating sheep coccidiosis, but their use will bring drug resistance, toxic side effects, drug residues, and other problems. Chinese herbal medicines are investigated as alternative methods for controlling coccidian infections.

Methods: In this study, the effect of fermented (FA) on oocysts per gram (OPG), average daily gain (ADG), and expression of inflammatory factors were investigated in lambs that were naturally infected with coccidia.

Results: The results showed that the FA had similar anti-coccidiosis effect to the original drug, while the FA demonstrated a more significant effect on weight gain, and a better ability to reduce the inflammatory response compared to the unfermented drug during the treatment period ( < 0.05). Furthermore, High-throughput sequencing technology was used to study the effects of FA on intestinal microbiota, and fecal metabolites of naturally infected lambs. The species richness of intestinal microbiota of lambs was significantly improved by FA. The abundance of bacteria , and were increased by fermentation of . The abundance of bacteria , , and was reduced. The prevention, and treatment of coccidiosis by fermentation of may also be related to a series of metabolites affected by intestinal microbiota, including artemisinin, Lysyl-Proline, and TRP-tyrosine.

Conclusion: FA was found to have superior anti-coccidiosis, anti-inflammatory, and weight gain effects compared to the original . Intestinal microbes and metabolites such as , , and Artemisinin were identified, suggesting their potential significance. was proposed as a biomarker for predicting intestinal coccidia outbreak risk in lambs, pending further validation. The correlation between microbiota, and metabolites may provide new insights into pathogenic changes associated with spp.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11747653PMC
http://dx.doi.org/10.3389/fcimb.2024.1448516DOI Listing

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